More jobs:
Expert Vendor Qualification
Job in
3000, Bern, Canton de Berne, Switzerland
Listed on 2026-09-13
Listing for:
CTC Resourcing Solutions
Full Time
position Listed on 2026-09-13
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Data Scientist
Job Description & How to Apply Below
CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.
Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases and other rare diseases.
For their site in Bern, Switzerland, our client is current looking for a:
Expert Vendor Qualificationon a 6-month contract, with possibilities of extension.
Main responsibilities:- Execute GxP supplier qualification activities.
- Lead vendor qualification including document review and audit execution.
- Ensure qualification of vendors providing GxP-relevant equipment and services.
- Act as Quality Delegate / Change Coordinator for Vendor Qualification Change Controls.
- Establish and Maintain Overview of already Qualified and to be Qualified Vendors.
- Relevant working/residency permit or Swiss/EU-Citizenship required.
- A Degree in life sciences and/or engineering.
- At least 5 years of experience as professional in the pharmaceutical industry or equivalent combination of education and experience.
- Demonstrated experience in quality assurance and regulatory compliance with GxP, Swiss medic, US FDA, TGA, EU, and other regulatory agency guidelines and in manufacturing of biologics.
- Direct experience in quality oversight of GxP-compliant vendor qualification processes, including planning, documentation review, and audit execution.
- Deep knowledge of GMP and global regulatory requirements, e.g. GMP, FDA, EU and other relevant GxP regulations.
- Effective collaboration with internal and external stakeholders.
- Fluent in English (spoken and written).
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